Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry

Abstract

Simple, straightforward and optimized procedures for preparing extended pi-conjugated linkers are described. Either unsubstituted or 4-donor substituted pi-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl pi-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki-Miyaura or Sonogashira coupling reactions.

DOI: 10.3762/bjoc.5.11

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Cite this paper

@inproceedings{Kulhanek2009ConvenientMF, title={Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry}, author={Jiri Kulhanek and Filip Bure{\vs} and Miroslav Ludwig}, booktitle={Beilstein journal of organic chemistry}, year={2009} }